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肿瘤抑制因子REIC/DKK-3与共伴侣蛋白SGTA:它们在雄激素敏感性中的相互作用及作用

Tumor suppressor REIC/DKK-3 and co-chaperone SGTA: Their interaction and roles in the androgen sensitivity.

作者信息

Ochiai Kazuhiko, Morimatsu Masami, Kato Yuiko, Ishiguro-Oonuma Toshina, Udagawa Chihiro, Rungsuriyawiboon Oumaporn, Azakami Daigo, Michishita Masaki, Ariyoshi Yuichi, Ueki Hideo, Nasu Yasutomo, Kumon Hiromi, Watanabe Masami, Omi Toshinori

机构信息

Department of Veterinary Nursing and Technology, School of Veterinary Science, Nippon Veterinary and Life Science University, Tokyo 180-8602, Japan.

Laboratory of Laboratory Animal Science and Medicine, Department of Disease Control, Graduate School of Veterinary Medicine, Hokkaido University, Sapporo 060-0818, Japan.

出版信息

Oncotarget. 2016 Jan 19;7(3):3283-96. doi: 10.18632/oncotarget.6488.

Abstract

REIC/DKK-3 is a tumor suppressor, however, its intracellular physiological functions and interacting molecules have not been fully clarified. Using yeast two-hybrid screening, we found that small glutamine-rich tetratricopeptide repeat-containing protein α (SGTA), known as a negative modulator of cytoplasmic androgen receptor (AR) signaling, is a novel interacting partner of REIC/DKK-3. Mammalian two-hybrid and pull-down assay results indicated that the SGTA-REIC/DKK-3 interaction involved the N-terminal regions of both REIC/DKK-3 and SGTA and that REIC/DKK-3 interfered with the dimerization of SGTA, which is a component of the AR complex and a suppressor of dynein motor-dependent AR transport and signaling. A reporter assay in human prostate cancer cells that displayed suppressed AR signaling by SGTA showed recovery of AR signaling by REIC/DKK-3 expression. Considering these results and our previous data that REIC/DKK-3 interacts with the dynein light chain TCTEX-1, we propose that the REIC/DKK-3 protein interferes with SGTA dimerization, promotes dynein-dependent AR transport and then upregulates AR signaling.

摘要

REIC/DKK-3是一种肿瘤抑制因子,然而,其细胞内的生理功能和相互作用分子尚未完全阐明。通过酵母双杂交筛选,我们发现富含谷氨酰胺的小四肽重复序列蛋白α(SGTA),已知为细胞质雄激素受体(AR)信号的负调节剂,是REIC/DKK-3的新型相互作用伙伴。哺乳动物双杂交和下拉试验结果表明,SGTA-REIC/DKK-3相互作用涉及REIC/DKK-3和SGTA的N端区域,并且REIC/DKK-3干扰了SGTA的二聚化,SGTA是AR复合物的一个组成部分,也是动力蛋白依赖性AR转运和信号传导的抑制剂。在人前列腺癌细胞中进行的报告基因试验显示,SGTA抑制了AR信号传导,而REIC/DKK-3的表达则使AR信号传导恢复。考虑到这些结果以及我们之前关于REIC/DKK-3与动力蛋白轻链TCTEX-1相互作用的数据,我们提出REIC/DKK-3蛋白干扰SGTA二聚化,促进动力蛋白依赖性AR转运,进而上调AR信号传导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/955b/4823106/2f24cbff9d76/oncotarget-07-3283-g001.jpg

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